Identification of Hen Egg Yolk-Derived Phosvitin ... - ACS Publications

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Identification of Hen Egg Yolk-Derived Phosvitin Phosphopeptides and Their Effects on Gene Expression Profiling against Oxidative Stress-Induced Caco-2 Cells Denise Young,† Franc-oise Nau,‡ Maryvonne Pasco,‡ and Yoshinori Mine*,† † ‡

Department of Food Science, University of Guelph, Guelph, Ontario N1G 2W1, Canada UMR 1253 INRA-Agrocampus Rennes Sciences et Technologie du Lait et de l’Oeuf, 65 rue de Saint Brieuc, 35042 Rennes Cedex, France ABSTRACT: Oxidative stress is involved in the initiation and propagation of chronic intestinal pathologies. Bioactive peptides such as egg yolk-derived phosvitin phosphopeptides (PPP3) have been previously shown to reduce in vitro oxidative stress by upregulating glutathione synthesis and antioxidant enzyme activities. Peptide and gene expression profile analysis of the PPP3 peptides can provide insight into structures involved in signal transduction mechanisms in the antioxidative stress response. The objectives of this research were to identify the PPP3 amino acid sequences before and after simulated gastrointestinal digestion and to assess the genes influenced by PPP3. Peptide sequences were analyzed using ESI Q-TOF-MS/MS, and the expression profile of 84 human oxidative stress and antioxidant defense genes were analyzed. Undigested PPP3 was composed of three main peptides: GTEPDAKTSSSSSSASSTATSSSSSSASSPNRKKPMDE (phosvitin-PV residues 441), NSKSSSSSSKSSSSSSRSRSSSKSSSSSSSSSSSSSSKSSSSR (PV residues 155197), and EDDSSSSSSSSVLSKIWGRHEIYQ (PV residues 244257) and their fragments. There was limited degradation of PPP3 after gastrointestinal digestion as deduced from the fragment sizes of digested PPP3, which ranged from 5 to 32 amino acids. These fragments were rich in contiguous serines and, in some cases, monoesterified with phosphate. Both undigested and digested PPP3 significantly reduced IL-8 secretion in H2O2-induced Caco-2 cells, indicating that antioxidative stress bioactivity is retained upon digestion. After PPP3 pretreatment, antioxidant genes associated with oxygen and reactive oxygen species (ROS) metabolism and cellular responses to chemical stimulus, oxidative stress, and ROS are upregulated in the presence and absence of oxidative stress, thereby contributing to the prevention of intestinal oxidative stress and the promotion of gut health. KEYWORDS: oxidative stress, phosvitin, phosphopeptides, mass spectrometry, PCR array, gene ontology, bioinformatics

’ INTRODUCTION An imbalance of reactive oxygen species (ROS) to antioxidants and oxidant detoxification systems can lead to oxidative stress and cellular damage. In the gastrointestinal tract, prolonged duration of high levels of oxidative stress could lead to the development or persistence of chronic conditions such as inflammatory bowel diseases, ischemic-reperfusion disorders, and intestinal cancer.1 Vitamin C, vitamin E, and endogenous antioxidants such as glutathione (GSH) and antioxidative stress enzymes such as catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione reductase (GR), and glutathione-S-transferase (GST) often act together to reduce oxidants and re-establish a stable redox balance. Although endogenous antioxidant mechanisms are triggered naturally in response to oxidative stress, some food-derived compounds have been shown to (1) further up-regulate glutathione synthesis by increasing the gene expression and activity of γ-glutamylcysteine synthetase (γ-GCS), (2) elevate GSH concentrations, and (3) increase the activities of antioxidative enzymes.25 The transcription of these genes is often linked to the nuclear response factor 2antioxidant response element (Nrf2-ARE) pathway,6 which is dependent on the release of Nrf2 from the cytosol, subsequent nuclear translocation, and binding to ARE in the promoter region of antioxidant genes. r 2011 American Chemical Society

Peptides isolated from phosvitin, a highly phosphorylated egg yolk protein with >50% serine residues, are found to exhibit a range of antioxidative stress properties. A bioactive fraction of phosvitin phosphopeptides, PPP3, reduced proinflammatory interleukin-8 (IL-8) secretion, lowered lipid peroxidation byproducts, increased intracellular GSH levels and γ-GCS mRNA activity, and elevated CAT, GR, and GST activities in H2O2induced Caco-2 intestinal cell culture.7,8 PPP3 is the third fraction of an anion-separated phosvitin hydrolysate, which was prepared by the alkaline hydrolysis and tryptic digestion of phosvitin.7 Of the three chromatographic separations, PPP3 was composed of the highest phosphorus and serine percentages of 18.9% (w/w) and possessed the highest bioactivity. Interestingly, phosvitin, o-phosphoserine, and dephosphorylated phosvitin peptides did not reduce IL-8 during in vitro oxidative stress.7 The PPP3 amino acid composition was determined, but provides limited insight on the peptide sequence and whether bioactivity is maintained after gastrointestinal digestion.

Received: May 25, 2011 Revised: July 29, 2011 Accepted: July 29, 2011 Published: July 29, 2011 9207

dx.doi.org/10.1021/jf202092d | J. Agric. Food Chem. 2011, 59, 9207–9218

Journal of Agricultural and Food Chemistry

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Table 1. Peptides Identified in Undigested PPP3 Using Nano-LC-MS/MS Mass Spectrometrya

a PPP3 was dephosphorylated prior to LC-MS/MS. Observed m/z values are obtained by mass spectrometry. Mr(expt) is the uncharged molecular mass of the peptide, and Mr(calc) is the theoretical mass of the closest matching peptide.

Phosvitin is resistant to gastrointestinal (GI) proteolysis9 partly due to the abundance of phosphate moieties. In the native protein, phosphate groups are largely monoesterified to serine and are arranged in blocks of up to 15 consecutive residues.10 PPP3, similar to most dietary proteins and peptides, is likely to undergo drastic structural changes during ingestion, digestion, and absorption. Proteinases such as pepsin, trypsin, and chymotrypsin in the gastrointestinal tract and brush-border peptidases at the surface of epithelial cells hydrolyze peptides to smaller increments.11 Therefore, the PPP3 peptide sequence and substrate specificities of the digestive enzymes will invariably influence the fragment sizes and the peptide’s functionality. In this study, we identify the peptides in undigested and pepsin- and pancreatin-digested PPP3 and assess the effect of PPP3 on an array of antioxidant and oxidant genes expressed during oxidative stress.

’ MATERIALS AND METHODS Materials. All reagents were purchased from Sigma-Aldrich Co. (St. Louis, MO) unless otherwise specified. PPP3 Preparation Method. The PPP3 fraction was isolated from the crude phosvitin phosphopeptide (PPPs) mixture using anionexchange high-performance liquid chromatography (HPLC) according to the procedure of Katayama et al.8 Briefly, PPPs were injected into a Mono Q HR 5/5 anion exchange column (Pharmacia Biotech, Uppsala, Sweden) and eluted with 20 mM ammonium bicarbonate with a linear NaCl gradient from 0 to 1.0 M. Three fractions were collected, and the last fraction, PPP3, was subsequently dialyzed using a 500 kDa MWCO membrane (Spectrum Laboratories Inc., Rancho Dominguez, CA) and freeze-dried. Simulated Gastrointestinal Digestion of PPP3. Human digestion of PPP3 was simulated in vitro using pepsin and pancreatin. To prepare the digested PPP3, PPP3 (5 mg) was first dissolved in 100 μL of 0.15 N HCl (pH 1.5). Porcine pepsin (EC 3.4.23.1, 3210 U/mg protein, SigmaAldrich) was added at an enzyme/substrate ratio of 1:250 (w/w), and the mixture were incubated at 37 °C for 2 h. KH2PO4 (50 μL, 0.5 M) and pancreatin (Sigma-Aldrich) at an enzyme/substrate ratio of 1:50 (w/w) were incorporated, and the solution was incubated at 37 °C for 8 h at pH 8.0. The digestion was terminated by heating at 90 °C for 5 min. PPP3 Dephosphorylation. PPP3 and digested PPP3 were combined with phosphatase (E:S = 1:25) prepared in a 10 mM potassium acetate/ acetic acid buffer (pH 5.2) and incubated for 8 h at 37 °C. After

incubation, the enzyme was inactivated at 80 °C for 10 min. Free phosphates and salts in the dephosphorylated samples were removed by dialysis for two consecutive days with daily changes of water using a 500 Da cutoff membrane (Spectrum Laboratories Inc.). Samples were then freezedried and rehydrated just prior to mass spectrometry analysis. Peptide Identification by ESI Q-TOF-MS/MS. Native and digested PPP3 peptide sequence analysis was performed at the mass spectrometry facility, Institut National Superieur de Formation Agroalimentaire (INSFA, Agrocampus Rennes, Rennes, France). All mass spectra of intact oligopeptides were obtained using matrix-assisted laser ionization/desorption time-of-flight (MALDI-TOF) configuration with a Voyager DE STR spectrometer (Applied Biosystem, Courtaboeuf, France) equipped with a nitrogen laser (337 nm, 20 Hz). All nanoelectrospray mass spectrometry (nES-MS) experiments for peptide mapping were conducted on a Q-TOF hybrid quadrupole/time-of-flight instrument (Micromass, Manchester, U.K.), for high resolution and online liquid chromatographytandem mass spectrometry (LC-MS/ MS) analyses. An external calibration was first performed in the range of 5003000 Da. The monoisotopic mass lists were compared to the proteomic server (http://us.expasy.org/) using Protein prospector software (http://prospector.ucsf.edu/) for peptide mass fingerprinting (PMF) analysis. The list of peptide masses was searched against the nonredundant protein sequence database provided by the National Center for Biotechnology Information (NCBI) server (http://www. ncbi.nlm.nih.gov). Cell Culture. The Caco-2 human intestinal cell line (American Type Culture Collection, Rockville, MD) was used in all in vitro oxidative stress studies. Cells were grown in Dulbecco’s modified Eagle’s medium/F12 (DMEM/F12; Gibco, Burlington, ON, Canada) supplemented with 20% fetal bovine serum (FBS; Hyclone, Logan, UT) and 50 units/mL of penicillinstreptomycin (Gibco) and were incubated at 37 °C in a 5% CO2 chamber. Cell passages 1545 were used to form the confluent monolayers required for the in vitro experiments. Monolayers were formed from 2 105 cells, which were grown for 57 days with fresh medium replacements every 23 days. Evaluation of Antioxidative Stress Activity in Vitro. Confluent Caco-2 cells in 48-well culture plates (Corning Costar, Cambridge, MA) were incubated for 2 h with PPP3 and digested PPP3 dissolved in DMEM/F12 medium containing 5% FBS, at 0.05 and 0.5 mg/mL. H2O2 was added at 1 mM, and cells were cultured for an additional 6 h. Culture supernatants were collected and stored at 80 °C for use in the IL-8 assays. 9208

dx.doi.org/10.1021/jf202092d |J. Agric. Food Chem. 2011, 59, 9207–9218


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Table 2. Peptides Identified in PPP3 Digested with Pepsin and Pancreatina

a

The peptide preparation was dephosphorylated prior to LC-MS/MS. Observed m/z values are obtained by mass spectrometry. Mr(expt) is the uncharged molecular mass of the peptide, and Mr(calc) is the theoretical mass of the closest matching peptide.

Figure 1. (A) Total ion chromatogram of the undigested PPP3 peptide, GTEPDAKTSSSSSSASSTATSSSSSSASSPNRKKPMD (positions 11151151). (B) Mass spectrum of a selected ion with m/z 378.12. Ions with (C) m/z 902.9038 and (D) m/z 1203.8712 were further fragmented, resulting in the respective MS/MS spectra. Peptides were detected by nanoelectrospray mass spectrometry coupled to a Q-TOF hybrid quadrupole/ time-of-flight instrument and online liquid chromatographytandem mass spectrometry. Interleukin-8 Assay. To measure IL-8 concentrations in cell culture supernatants, 96-well microtiter plates were coated overnight at 4 °C with 0.05 μg/well mouse anti-human IL-8 antibody (BD Biosciences, San Diego, CA) in 100 mM sodium phosphate buffer (PBS), pH 9.0. Plates were blocked with PBS containing 1% (w/v) bovine serum albumin (BSA) (Thermo Fisher Scientific, Inc., Waltham, MA), followed by the addition of culture supernatants and IL-8 standards diluted in PBS containing 0.05% (v/v) Tween-20 (PBST; Thermo Fisher) and 1% BSA. Bound IL-8 was detected using biotinylated mouse anti-human IL-8 antibody (0.025 μg/well; BD Biosciences), followed by avidinconjugated horseradish peroxidase (1:2000; BD Biosciences) diluted in PBST containing 1% BSA, and visualized using 3,30 ,5,50 -tetramethylbenzidine (Sigma-Aldrich). The reaction was stopped using 1 M H2SO4,

and the absorbance was read at 450 nm. IL-8 concentrations in the samples were determined from the IL-8 standard curve and expressed as picograms of IL-8 per milliliter of sample. Influence of PPP3 on Antioxidant Gene Expression. Confluent Caco-2 cells were incubated in a 5% FBS-DMEM/F12 medium with 1 mg/mL of PPP3 for 2 h. H2O2 (1 mM) was added to the cells to induce oxidative stress for 1 h. At the end of 3 h, the cells were rinsed with PBS, and mRNA was extracted and synthesized into cDNA for RT-PCR. Isolation of RNA and Reverse Transcription. Total RNA was extracted from adherent cultured cells using the Aurum Total RNA Mini Kit (Bio-Rad Laboratories). After the microtiter wells had been rinsed with PBS, lysis buffer (350 μL) was added to each well. Cell lysates 9209


Journal of Agricultural and Food Chemistry (200 μL) were transferred into new eppendorf tubes and mixed with equal volumes of 70% ethanol. The entire volume was transferred into the RNA binding column fitted into a 2 mL capless tube. The remaining steps were conducted in accordance with the manufacturer’s instructions. The quantity and quality of the RNA was verified by measuring the A260 and A280 (NanoDrop ND-1000; Thermo Scientific, Wilmington, DE) and by gel electrophoresis. First-strand cDNA was synthesized using the RT2 First Strand Kit (SA Biosciences, Frederick, MD) according to the manufacturer’s instructions. Oxidative Stress and Antioxidant Defense PCR Array. The mRNA expression of a wide range of genes related to oxidative stress was quantified using RT-PCR with the RT2 Profiler PCR Array: human oxidative stress and antioxidant defense. RT-PCR was carried out using the High Performance RT2 qPCR Master Mixes (SA Biosciences) on a MyiQ Single Color Real-Time PCR Detection System (Bio-Rad Laboratories) using the following conditions: denaturation, 15 s at 95 °C; annealing, 15 s at 56 °C; and extension, 30 s at 72 °C. Signaling Pathway Analysis. Fold up- or down-regulation was calculated relative to untreated control cells, and a gene was considered to be differentially expressed when it had a fold change of at least (1.5. Gene ontology (GO) analysis was carried out using GoMiner.12 A GO biological process was considered to be enriched when the Fisher’s exact p value was e0.05. Functional pathway and network analyses were generated through the use of Ingenuity pathway analysis (version 2.0, Ingenuity Systems, Mountain View, CA). Ingenuity pathway analysis identified canonical pathways, biological processes, and gene interaction networks that were most significant to the gene expression data from the PCR array. Statistical Analysis. All analyses were performed in triplicate unless specified otherwise. Statistical analyses were carried out using GraphPad (San Diego, CA) software. The statistical significance was determined by the Student’s t test with a P e 0.05 taken as significant. Groups were considered to be statistically significant when P e 0.05. Results are reported as the mean ( SEM.

’ RESULTS AND DISCUSSION Antioxidants have been shown to alleviate and suppress chronic intestinal diseases such as cancer and inflammatory bowel disease in vivo.1315 The GI tract is susceptible to ingested food compounds such as transition metal ions, heme, isoprostanes, additives, and lipids and their oxidized products.16 These components act as oxidants, contributing to the ROS burden from endogenous and exogenous sources. Antioxidative stress compounds such as egg yolk-derived phosvitin phosphopeptides (PPP3)7 may prevent the establishment of intestinal disease because they contribute to the up-regulation of endogenous antioxidant enzymes and glutathione synthesis in the epithelium. Bioactive peptides in PPP3 were identified and were compared with PPP3 peptides after simulated gastrointestinal digestion. All peptides were identified as originating from the parent phosvitin region of vitellogenin II (UniProtKB/Swiss-Prot P02845, VIT2_CHICK), confirming the purity of the starting material for the phosphopeptide preparation. The PPP3 sample consisted of 13 identified peptides of 843 amino acid residues (Table 1), whereas digested PPP3 was made up of peptide fragments with 532 amino acids (Table 2). Three major PPP3 peptides emerged with the other 10 remaining peptides consisting of shorter fragments within these major sequences: GTEPDAKTSSSSSSASSTATSSSSSSASSPNRKKPMDE (PV residues 441); NSKSSSSSSKSSSSSSRSRSSSKSSSSSSSSSSSSSSKSSSSR (PV residues 155197); and EDDSSSSSSSSVLSKIWGRHEIYQ (PV residues 244257). The total ion

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Figure 2. Effect of PPP3 and digested PPP3 (dPPP3) on IL-8 secretion in H2O2-treated Caco-2 cells. Cells were treated with 0.05 or 0.5 mg/mL of peptides for 2 h at 37 °C and then incubated with 1 mM H2O2 for 6 h. Data are presented as the mean ( SEM; n = 3. P e 0.05 compared to H2O2-treated cells.

Figure 3. Differentially expressed genes and GO biological processes. (A) Genes were differentially expressed (P e 0.05) in H2O2, PPP3 followed by H2O2 (PPP3), and PPP3 alone (PPP3C). Cells were treated with 0.5 mg/mL of peptides for 2 h at 37 °C and then incubated with 1 mM H2O2 for 1 h. A total of 14 overlapping genes were commonly expressed among all three groups. (B) Gene ontology (GO) biological processes significantly enriched (P e 0.05) with the genes from H2O2, PPP3, and PPP3C treatments. Only one overlapping biological process was commonly enriched among all three groups.

chromatogram and an example of fragmentation spectra of a PPP3 peptide fragment (positions 11151151) are shown in Figure 1; other PPP3 peptides were identified in the same manner. Many pepsin- and pancreatin-digested peptide fragments were found within the PPP3 peptide sequence such as the 5 digested peptides within PPP3 (PV residues 441) and 6 digested peptides within PPP3 (PV residues 244257). Unfortunately, digested fragments from PV 155197 residues were not detected. Although these sequences were not identified in PPP3, it is likely due to difficulties in ionization rather than the absence of the peptide in the mixture due to highly monophosphorylated serine residues. The substrate specificities of the digestive enzymes and the amino acid sequence of the original PPP3 preparation influence the size and sequence of digested peptides. Hydrolysis with pepsin generates peptides containing Y, F, or L in the N-terminal positions.17 After pepsin digestion in the stomach, a mixture of 9210



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Figure 4. GO biological processes significantly (P e 0.05) enriched with genes from (A) H2O2, (B) PPP3, and (C) PPP3C groups. Up-regulated processes are highlighted in bold and downregulated processes are in lightface text.

pancreatic peptidases in the small intestine further cleaves oligopeptides into smaller fragments. Pancreatin is composed of the endopeptidases trypsin, R-chymotrypsin, and elastase

and the exopeptidases carboxypeptidases A and B, with trypsin and chymotrypsin predominantly responsible for the majority of digestion in the duodenum. Because trypsin cleaves at the 9211



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carboxyl side of arginine or lysine18,19 and PPP3 is prepared from the tryptic hydrolysis of phosvitin, peptides NSKSSSSSSKSSSSSSRSRSSSKSSSSSSSSSSSSSSKSSSSR and EDDSSSSSSSSVLSKIWGRHEIYQ are generated. Further tryptic digestion of PPP3 resulted in the identification of additional peptides of which two and three peptides have C-terminal arginine and lysine, respectively. Interestingly, when the GI-digested PPP3 sequences are compared with that of PPP3 and native phosvitin, tryptic hydrolysis occurs after amino acids that are not directly adjacent to contiguous serines. The steric hindrance created by the contiguous phosphorylated serines and the anionic character of the phosphate moieties likely conferred a marked resistance to the action of digestive enzymes. Oligopeptides are capable of crossing the intestinal barrier and entering the bloodstream,20,21 but post-translational modifications such as phosphorylation can affect peptide transport. Phosphopeptides have poor cell penetration because the negatively charged phosphate moieties are poorly transported across the cell membrane.22 Even after simulated physiological digestion, digested PPP3, like pepsin- and pancreatin-digested casein phosphopepitdes (CPP), retain a high degree of phosphorylation.23 Therefore, it is likely that these phosphorylated peptides exert bioactivity in the gut lumen or through receptors on the intestinal epithelial cells.11 Using Caco-2 human epithelial cells, we demonstrated that both undigested and digested PPP3 at 0.05 mg/mL and at 0.05 and 0.5 mg/mL, respectively, significantly reduced the H2O2-stimulated secretion of IL-8 (Figure 2). It is therefore plausible that after PPP3 consumption, digested PPP3 contributes to the reduction of oxidative stress in the epithelium. Contiguous serine and phosphoserine sequences are prevalent in the identified PPP3 peptides and may influence bioactivity. The majority of PPP3 peptides possess at least two contiguous serines, and SerSer was found in all digested peptides. About 96% of seryl residues in phosvitin are phosphorylated,24 and phosphorylated peptides were identified in both PPP3 and digested PPP3 preparations (Tables 1 and 2). The CPP sequence, SerPSerPSerPGluGlu, is believed to present

a polar, acidic region ideal for sequestering ferrous ion and quenching free radicals.25 Although this effect is largely attributed to the phosphate groups in the phosphorylated serine residues, free phosphate and phosphoserine have a lower effect against oxidation compared to phosphorylated caseins.26 Phosvitin phosphopeptides also have strong antioxidant capacities,27 but whereas PPP3 influenced GSH and antioxidant enzyme pathways, serine and o-phosphoserine did not affect antioxidative stress activity.7 These results suggest that contiguous phosphoserine sequences may interact with apical cell surface receptors and signal the enhancement of detoxification and antioxidant enzymes. Gene ontology (GO) analysis was used to determine the biological roles and molecular functions of the differentially expressed genes in Caco-2 cells pretreated with PPP3 and stimulated with H2O2. Fold up- or down-regulation was calculated relative to untreated control cells, and expression was considered to be biologically significant if a fold change of 1.5 or greater was observed. Of the biologically significant up-/downregulated genes observed, a total of 21 genes were differentially expressed in H2O2-stressed cells with 20 genes up-regulated and 1 gene down-regulated (Figure 3A) and corresponded to 2 upregulated GO biological processes (Figure 3B): immune response [GO:0006955] and oxygen and reactive oxygen species metabolic process [GO:0006800] (Figure 4A). PPP3-treated oxidatively stressed cells revealed 53 differentially expressed genes with 35 genes up-regulated and 18 genes down-regulated. Thirteen GO processes were significantly enriched, with 4 biological processes up-regulated: oxygen and ROS metabolic process [GO:0006800], cellular response to chemical stimulus [GO:0070887], cellular response to oxidative stress [GO:0034599], and cellular response to ROS [GO:0034614]. Down-regulated GO processes were related to cellular metabolic processes (Figure 4B). Although PPP3 control cells were not exposed to oxidant, 52 genes were differentially expressed, with 40 upregulated and 12 down-regulated genes that comprised 25 upregulated and 1 down-regulated GO biological process. Similar to the 4 up-regulated processes in PPP3, PPPC also up-regulated responses to ROS [GO:0000302] and hydrogen peroxide

Table 3. Gene Ontology (GO) Biological Processes Commonly Enriched with Genes Differentially Expressed in Caco-2 Cells in Response to H2O2 Stimulation, PPP3 Pretreatment and H2O2 Stimulation, and PPP3 Alone (PPP3C)a H2O2

PPP3

GO process

genes

P value

oxygen and reac-

PREX1, NOX5, NCF1,

0.005

genes GPX3, NOX5, PRDX3,

PPP3C P value 0.03

genes GPX3, DUOX1, NOX5, PRDX3,

tive oxygen

LPO, EPX, EPHX2,

SOD2, NCF1, LPO,

species meta-

PRG3, PXDNL,

EPX, EPHX2, BNIP3,

CCS, EPX, GPX4, BNIP3,

bolic process

NOS2, MPO,

SFTPD, TPO, PRDX1,

SFTPD, TPO, PRDX1, NOS2,

[GO:0006800]

DUOX2, PXDN,

NOS2, MPO, DUOX2,

MPO, DUOX2, AOX1, PXDN,

NCF2 (13/32)

AOX1, PXDN, NCF2

NCF2 (21/32)

P value 0.009

SOD2, NCF1, ALOX12, LPO,

(18/32) a

Numbers in parentheses after the gene listing indicate the number of up-regulated genes relative to the total number of genes in the category. Genes in bold text indicate genes differentially expressed in PPP3 and PPP3C treatments that are absent during H2O2 stimulation alone. Italicized genes are unique to H2O2-stressed cells within the GO biological process. Genes are abbreviated as follows: ALOX12, arachidonate 12-lipoxygenase; AOX1, aldehyde oxidase 1; BNIP3, BCL2/adenovirus E1B 19 kDa interacting protein 3; CCS, copper chaperone for superoxide dismutase; DUOX1, dual oxidase 1; DUOX2, dual oxidase 2; EPHX2, epoxide hydrolase 2, cytoplasmic; EPX, eosinophil peroxidase; GPX3, glutathione peroxidase 3 (plasma); GPX4, glutathione peroxidase 4 (phospholipid hydroperoxidase); LPO, lactoperoxidase; MPO, myeloperoxidase; NCF1, neutrophil cytosolic factor 1; NCF2, neutrophil cytosolic factor 2; NOS2, nitric oxide synthase 2, inducible; NOX5, NADPH oxidase, EF-hand calcium binding domain 5; PRDX1, peroxiredoxin 1; PRDX3, peroxiredoxin 3; PREX1, phosphatidylinositol-3,4,5-trisphophate-dependent Rac; PRG3, proteoglycan 3; PXDN, peroxidasin homologue (Drosophila); PXDNL, peroxidasin homolog (Drosophila)-like; SFTPD, surfactant protein D; SOD2, superoxide dismutase 2; and TPO, thyroid peroxidase. 9212



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Table 4. Gene Ontology (GO) Biological Processes Commonly Enriched with Genes Differentially Expressed in Caco-2 Cells in Response to PPP3 Pretreatment and H2O2 Stimulation and PPP3 Alone (PPP3C)a PPP3 genes

P value

SFTPD, GPX3, PRDX5, TPO, PRDX1,

0.03

GO process cellular response to

PPP3C P value

genes GPX3, DUOX1, PRDX3, LPO, EPX,

chemical stimulus

PRDX3, DUOX2, LPO, MPO,

GPX4, SFTPD, PRDX5, TPO, SELS,

[GO:0070887]

PXDN, EPX (11/17)

PRDX1, MPO, DUOX2, PXDN (14/ 17)

cellular response to oxidative stress

GPX3, PRDX5, TPO, PRDX1, PRDX3,

0.03

DUOX2, LPO, MPO, PXDN, EPX

[GO:0034599]

GPX3, PRDX5, DUOX1, TPO, PRDX1,

0.001

0.005

PRDX3, DUOX2, LPO, MPO, PXDN, EPX, GPX4(12/15)

(10/15)

cellular response to reac-

GPX3, PRDX5, TPO, PRDX1, PRDX3,

tive oxygen species

DUOX2, LPO, MPO, PXDN, EPX

PRDX3, DUOX2, LPO, MPO,

[GO:0034614]

(10/15)

PXDN, EPX, GPX4(12/15)

0.03

GPX3, PRDX5, DUOX1, TPO, PRDX1,

0.005

a

Numbers in parentheses after the gene listing indicate the number of up-regulated genes relative to the total number of genes in the category. Genes in bold text indicate genes differentially expressed in PPP3 control cells that are absent during PPP3-treated and H2O2-stimulated cells. Genes are abbreviated as follows: DUOX1, dual oxidase 1; DUOX2, dual oxidase 2; EPX, eosinophil peroxidase; GPX3, glutathione peroxidase 3 (plasma); GPX4, glutathione peroxidase 4 (phospholipid hydroperoxidase); LPO, lactoperoxidase; MPO, myeloperoxidase; PRDX1, peroxiredoxin 1; PRDX3, peroxiredoxin 3; PRDX5, peroxiredoxin 5; PXDN, peroxidasin homolog (Drosophila); SELS, selenoprotein S; SFTPD, surfactant protein D; SOD2, superoxide dismutase 2; and TPO, thyroid peroxidase.

Table 5. Biologically Significant Up- and Down-regulated Genes Related to Oxygen and Reactive Oxygen Species (ROS) Metabolism and Cellular Responses to Chemical Stimulus, Oxidative Stress, and ROSa fold change gene symbol

accession no.

gene description

H2O2

PPP3

PPP3C 3.35 3.18

ALOX12 AOX1

NM_000697 NM_001159

arachidonate 12-lipoxygenase aldehyde oxidase 1

1.09 1.33

1.33 2.90

BNIP3

NM_004052

BCL2/adenovirus E1B 19 kDa interacting protein 3

1.01

1.76

2.82

CCS

NM_005125

copper chaperone for superoxide dismutase

1.13

1.10

1.56

DUOX1

NM_175940

dual oxidase 1

1.38

1.01

1.82

DUOX2

NM_014080

dual oxidase 2

1.51

3.48

4.33

EPHX2

NM_001979

epoxide hydrolase 2, cytoplasmic

2.38

2.33

1.13

EPX

NM_000502

eosinophil peroxidase

3.23

4.14

3.98

GPX3 GPX4

NM_002084 NM_002085

glutathione peroxidase 3 (plasma) glutathione peroxidase 4 (phospholipid hydroperoxidase)

1.12 1.02

2.05 1.32

2.13 1.56

LPO

NM_006151

lactoperoxidase

15.70

19.89

4.32

MPO

NM_000250

myeloperoxidase

8.33

16.44

27.59

NCF1

NM_000265

neutrophil cytosolic factor 1

3.45

4.96

4.57

NCF2

NM_000433

neutrophil cytosolic factor 2

2.38

3.52

3.73

NOS2

NM_000625

nitric oxide synthase 2, inducible

3.29

9.38

10.49

NOX5

NM_024505

NADPH oxidase, EF-hand calcium binding domain 5

2.86

3.05

3.73

PRDX1 PRDX3

NM_002574 NM_006793

peroxiredoxin 1 peroxiredoxin 3

1.19 1.35

1.58 4.40

1.51 3.60

PRDX5

NM_181652

peroxiredoxin 5

1.14

1.59

1.66

PREX1

NM_020820

phosphatidylinositol-3.4,5-trisphophate-dependent Rac

3.82

1.17

1.19

PRG3

NM_006093

proteoglycan 3

2.22

3.63

1.63

PXDN

NM_012293

peroxidasin homologue (Drosophila)

2.76

6.45

4.65

PXDNL

NM_144651

peroxidasin homologue (Drosophila)-like

5.14

1.06

1.00

SELS

NM_203472

selenoprotein S

1.19

1.33

1.76

SFTPD SOD2

NM_003019 NM_000636

surfactant protein D superoxide dismutase 2

1.09 1.14

2.81 1.94

1.56 2.14

TPO

NM_000547

thyroid peroxidase

1.34

2.05

2.28

Genes are annotated using GenBank accession numbers. Fold change values g +1.5 or e 1.5 were chosen as cutoff values, defining increased and decreased expression, respectively. Up-regulated fold change values are highlighted in bold. a

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Journal of Agricultural and Food Chemistry [GO:0042542 and GO:0042744], cellular response to stimulus [GO:0051716] and stress [GO:0033554], cell surface receptor linked signal transduction [GO:0007166], and general cellular localization, cell death, and catabolic and developmental processes (Figure 4C), with the exception of the amine metabolic process [GO:0009308], which was the only GO down-regulated process. These analyses indicate a strong response to oxygen and ROS, and indeed, this metabolic process [GO:0006800] was the most significant overlapping enriched GO biological process among the three treatments. Responses to oxidants, ROS, and chemical stimulus were even more enhanced in PPP3 and PPP3treated without H2O2 (PPP3C) groups, suggesting PPP3 may

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play a major role in the detoxification of H2O2 via attachment to cell surface receptors. In the absence of oxidant, PPP3C cells also influenced apoptosis and cellular death biological processes; however, as both negatively [GO:0043066; GO:0043069; and GO:0060548] and positively [GO:0010941; GO:0042981; and GO:0043067] regulated processes were enriched, this may be indicative of cellular homeostasis maintenance. The differentially expressed genes uniquely associated with H2O2 stimulation included PREX1 (phosphatidylinositol-3,4, 5-triphosphate-dependent Rac), NCF1 (neutrophil cytolsolic factor-1), PRG3 (proteoglycan-3), and PXDNL (peroxidasinlike protein precursor) (Table 3). Both NCF1 and PRG3 are

Figure 5. Continued 9214



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Figure 5. Continued

associated with superoxide production,28,29 PREX1 functions in superoxide metabolism,30 and PXDNL plays a role in phagocytosis and defense.31 ROS production and immune defense are closely linked, and the up-regulated CCL5 (chemotactic cytokine), which recruits T cells, eosinophils, basophils, and leukocytes to inflammation sites,32 within the enriched GO process [GO:0006955] is indicative of this. In comparison, PPP3 and PPP3C also influenced genes primarily involved in H2O2 and ROS detoxification such as GPX3, peroxiredoxin (PRDX1 and PRDX3), and SOD2, as well as a gene encoding a surfactant protein, SFTPD, which traps microorganisms and prevents oxidative stress and inflammation (Table 4).33 The three other

up-regulated genes, BNIP3, TPO, and AOX1, play roles in apoptosis, thryroid gland function, and oxidant formation, respectively.3436 PPP3 administered to cells in the absence of H2O2 also increased the expression of DUOX1, ALOX12, CCS, GPX4, and SELS in the GO processes associated with oxygen and ROS metabolism and in cellular responses to chemical stimulus, oxidative stress, and ROS (Table 5). Whereas dual oxidase 1 (DUOX1) and arachidonate 12-lipoxygenase (ALOX12) are associated with the production of ROS and inflammation,37,38 respectively, the copper chaperone for superoxide dismutase (CCS) and GPX4 have antioxidant functions.39 Selenoprotein S (SELS) may also play a role in regulating 9215



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Figure 5. Pathway analysis of mRNA differentially expressed in (A) H2O2, (B) PPP3, and (C) PPP3C groups compared with baseline Caco-2 cells. Cells were treated with 0.5 mg/mL of peptides for 2 h at 37 °C and then incubated with 1 mM H2O2 for 1 h. PCR array fold change results were input into the Ingenuity pathway analysis program, which mapped genes to a network with NFkB as the main node. Numbers under the network shapes indicate the associated fold change. Color shading corresponds to the type of deregulation: red for up-regulated genes and green for down-regulated genes. The color intensity reflects the degree of up- or down-regulation. White open nodes are not from among the PCR array gene list, but are proteins associated with the regulation of some of these identified genes. Continuous and discontinuous lines represent direct and indirect functional and physical interaction between genes from the literature.

cytokine production,40 suggesting that even PPP3 alone can have a profound influence in bolstering endogenous antioxidative defenses and preventing the development of inflammation. Network analyses showed that the PPP3 antioxidant upregulated pathways indirectly centered on the transcription factor, NFkB (Figure 5), which regulates genes related to immune

function, inflammation, apoptosis, and cell proliferation.41 Oxidants such as H2O2 can activate NFkB by phosphorylating inhibitor kB (IkB), releasing NFkB from the cytoplasm, and allowing its subsequent translocation into the nucleus where the transcription factor binds to and activates sequence-specific regions of DNA. It has been suggested that there is cross-talk between the 9216


Journal of Agricultural and Food Chemistry NFkB and Nrf2-ARE pathway, and several phytochemicals have been shown to suppress NFkB signaling while activating the antioxidative pathway.42,43 It is likely that PPP3 also function in a similar manner, culminating in reduced IL-8 secretion, as seen in vitro, and in up-regulated antioxidant genes such as GPX3, PRDX3, and SOD2 (Figure 5B,C). In conclusion, most of the peptides generated after PPP3 digestion in simulated GI are derived from the sequences identified in undigested PPP3. Digested PPP3 have antioxidative stress properties, and given the polyanionic nature of the peptides, they are likely retained in the gastrointestinal lumen, where they up-regulate antioxidative genes to prevent oxidative stress and promote gut health.

’ AUTHOR INFORMATION Corresponding Author

*Phone: (519) 824-4120, ext. 52901. Fax: (519) 824-6631. E-mail: [email protected].

’ ACKNOWLEDGMENT We thank the Advanced Foods and Materials Network (AFMNet), part of the Networks of Centres of Excellence (NCE), Canada for financially supporting this project. ’ ABBREVIATIONS USED PPP3, phosvitin phosphopeptides; ROS, reactive oxygen species; GSH, glutathione; CAT, catalase; SOD, superoxide dismutase; GPx, glutathione peroxidase; GR, glutathione reductase; GST, glutathione-S-transferase; γ-GCS, γ-glutamylcysteine synthetase; Nrf2-ARE, nuclear response factor 2antioxidant response element; IL-8, interleukin-8; H2O2, hydrogen peroxide; GI, gastrointestinal; FBS, fetal bovine serum; PBS, sodium phosphate buffer; BSA, bovine serum albumin; CPP, casein phosphopeptides; dPPP3, PPP3 digested with pepsin and pancreatin; LC, liquid chromatography; MS, mass spectrometry; NFkB, nuclear factor kB; IkB, inhibitor kB. ’ REFERENCES (1) Cao, W.; Vrees, M. D.; Kirber, M. T.; Fiocchi, C.; V.E. Pricolo, V. E. Hydrogen peroxide contributes to motor dysfunction in ulcerative colitis. Am. J. Physiol. Gastrointest. Liver Physiol. 2004, 286, G833–G843. (2) Masella, R.; Vari, R.; D’Archivio, M.; Di Benedetto, R.; Matarrese, P.; Malorni, W.; Scazzocchio, B.; Giovannini, C. Extra virgin olive oil biophenols inhibit cell-mediated oxidation of LDL by increasing the mRNA transcription of glutathione-related enzymes. J. Nutr. 2004, 134, 785–791. (3) Biswas, S. K.; McClure, D.; Jimenez, L. A.; Megson, I. L.; Rahman, I. Curcumin induces glutathione biosynthesis and inhibits NF-kB activation and interleukin-8 release in alveolar epithelial cells: mechanism of free radical scavenging activity. Antioxid. Redox Signal. 2005, 7, 32–41. (4) Molina, M. F.; Sanchez-Reus, I.; Iglesias, I.; Benedi, J. Quercetin, a flavonoid antioxidant, prevents and protects against ethanol-induced oxidative stress in mouse liver. Biol. Pharm. Bull. 2003, 26, 1398–1402. (5) Li, Y.; Cao, Z.; Zhu, H. Upregulation of endogenous antioxidants and phase 2 enzymes by the red wine polyphenol, resveratrol in cultured aortic smooth muscle cells leads to cytoprotection against oxidative and electrophilic stress. Pharmacol. Res. 2006, 53, 6–15. (6) Griffith, O. W. Biologic and pharmacologic regulation of mammalian glutathione synthesis. Free Radical Biol. Med. 1999, 27, 922–935.

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Identification of Hen Egg Yolk-Derived Phosvitin ... - ACS Publications

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